192,690 research outputs found
Naturalization record of Gonzalez, Bernardo L
No full textThe naturalization certificate for Bernardo L. Gonzalez of Spain. Signed by Judge Joseph B. Wall
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[Letter from Pedro J. Gonzalez to H. L. Cardoso, 2]
No full textLetter from Pedro J. Gonzalez to H. L. Cardoso. A long, curving title is printed above small lines of text that sit above and beside a bird icon, below which is a printed date and a stamped seal. A single wide column of text sits below the stamped seal and is positioned to the right of a smaller text column. The wide column of text continues onto the page's back and ends above a signature next to a second seal and a short paragraph printed above handwritten text
Gonzalez, Mary L.
No full textCentro Asturiano membership record of Mary L. Gonzalez; Socio Number: 1365.https://digitalcommons.usf.edu/asturiano_membership/3471/thumbnail.jp
Naturalization record of Gonzalez, Manuel
No full textThe naturalization certificate for Manuel Gonzalez of Cuba. Signed by Judge Henry L. Mitchell
Rumer's transformation: A symmetry puzzle standing for half a century
No full textIn 1966, only a few months after the complete elucidation of the standard nuclear genetic code (Kay, 2000), the Russian theoretical physicist Yury Borisovich Rumer uncovered the existence of a particular symmetry (Rumer, 1966): when the keto-amino transformation (also known as Rumer's transformation) is applied to the bases of a codon then the degeneracy of the transformed codon was changed. In particular, if the amino acid associated to the starting codon has degeneracy 4, then the amino acid associated to the transformed codon has degeneracy 1, 2 or 3 (and vice versa). After half a century from this discovery and despite the universality of Rumer's symmetry, little is known about its origin and its possible biological significance. In this article we show that Rumer's symmetry could have originated in an ancestral version of the genetic code, i.e., the pre-early code, and is a natural consequence of the stereo-chemical symmetries of the ancestral synthesis machinery working around such code (Gonzalez et al., 2019). Moreover, the conservation of Rumer's symmetry through evolutionary periods suggests a connection with key biological features. In this respect, intriguing possibilities include those of error detection/correction, control over the synthesis of proteins, and frame maintenance. To a certain extent, such ideas have been explored in the framework of a mathematical model of the genetic code (the non-power model of the genetic code (Gonzalez, 2004; Gonzalez, 2008; Gonzalez et al., 2016), whose definition of dichotomic classes naturally includes Rumer's symmetry (Gonzalez, 2008; Gonzalez et al., 2006, 2008) and the theory of circular codes (Arquès and Michel, 1996; Gonzalez et al., 2011; Fimmel et al., 2015)
Naturalization record of Gonzalez Rodriguez, Fernando
No full textThe naturalization certificate for Fernando Gonzalez Rodriguez of Spain. Signed by Judge Henry L. Mitchell
John L. Gonzalez
No full textThis black and white photograph is located in Halstead in 1951. John L. Gonzalez is wearing a white suit and is standing on a bridge in Halstead. The water in the background appears to be flood-stage on the river.https://scholars.fhsu.edu/harvey/1076/thumbnail.jp
Leioproctus (Perditomorpha) rosellae Gonzalez
No full textLeioproctus (Perditomorpha) rosellae Gonzalez in Gonzalez & Florez, 2011 (Figures 15–28) Diagnosis. Among species of the neotropicus group sensu Michener (2007), L. rosellae can easily be recognized by the following combination of characters: female inner metatibial spur with few, elongate branches; scutum in both sexes uniformly punctate, with coarse punctures separated by a puncture width or less (Figs. 15, 18); female metasomal terga largely impunctate, with minute, faint, scattered punctures, without integumental or apical hair bands (Fig. 17); body pubescence largely ferruginous in the female (Fig. 15), in the male restricted to pronotal lobe, scutum, and scutellum (Fig. 18); and female tibial scopa with sparse, long (2.5 –3.0 times median ocellar diameter), apically branched hairs. Description (Male). As in the female (cf. Gonzalez & Florez 2011), except: Body length 6.9 mm; forewing length 4.8 mm; head width 2.1 mm. Head 1.3 times wider than long; inner orbits of compound eyes converging below (Fig. 20); intertorular distance 2.3 times median ocellar diameter, 1.8 times length of torulorbital distance; torulus diameter slightly narrower (0.8 times) than median ocellar diameter; ocellocular distance 1.8 times median ocellar diameter; interocellar distance about 1.8 times median ocellar diameter; clypeus about 1.7 times broader than long; gena about 0.5 times width of compound eye in profile; scape 3.2 times longer than broad; antennal flagellum more than three times longer than scape; pedicel about as long as broad; first flagellomere about twice as long as second, slightly longer than third. Inner metatibial spur straight, ciliate as in outer spur. Sixth to eighth sterna and genital capsule as in figures 22–28. Color generally as in female except legs and metasoma largely dark brown to black. Pubescence shorter and sparser than in female, except as follows: clypeus and inferior paraocular area with dense, minutely branched, silver hairs; legs and metasoma with whitish hairs; discs of second and third metasomal terga with short (at most one-third median ocellar diameter), simple, erect hairs. Integument with coarser and denser punctures than in female, particularly on head and metasomal terga. Examined material. COLOMBIA: 3 Ƥ, 13, Magdalena, Santa Marta, on road from Bastidas to Bahía Concha, 11 º 15.874 ’N, 74 º 09.924W; Dec 18, 2011, 99 m., V.H. Gonzalez, P. Sepúlveda (ICN, SEMC). Comments. This species was previously known from the female holotype, which is in somewhat poor condition. The male of L. rosellae agrees in most characters with those of the female, except in the usual secondary sexual features, the shorter, sparser body pubescence and the integument with coarser and denser punctures, particularly on head and metasomal terga.Published as part of Gonzalez, Victor H., Sepúlveda, Paula A. & Griswold, Terry L., 2012, Taxonomic notes on American Heriades Spinola, 1808 and Leioproctus Smith, 1853 (Hymenoptera: Megachilidae, Colletidae), pp. 75-78 in Zootaxa 3591 on page 78, DOI: 10.5281/zenodo.21390
Leioproctus (Perditomorpha) rosellae Gonzalez
No full textLeioproctus (Perditomorpha) rosellae Gonzalez in Gonzalez & Florez, 2011 (Figures 15–28) Diagnosis. Among species of the neotropicus group sensu Michener (2007), L. rosellae can easily be recognized by the following combination of characters: female inner metatibial spur with few, elongate branches; scutum in both sexes uniformly punctate, with coarse punctures separated by a puncture width or less (Figs. 15, 18); female metasomal terga largely impunctate, with minute, faint, scattered punctures, without integumental or apical hair bands (Fig. 17); body pubescence largely ferruginous in the female (Fig. 15), in the male restricted to pronotal lobe, scutum, and scutellum (Fig. 18); and female tibial scopa with sparse, long (2.5 –3.0 times median ocellar diameter), apically branched hairs. Description (Male). As in the female (cf. Gonzalez & Florez 2011), except: Body length 6.9 mm; forewing length 4.8 mm; head width 2.1 mm. Head 1.3 times wider than long; inner orbits of compound eyes converging below (Fig. 20); intertorular distance 2.3 times median ocellar diameter, 1.8 times length of torulorbital distance; torulus diameter slightly narrower (0.8 times) than median ocellar diameter; ocellocular distance 1.8 times median ocellar diameter; interocellar distance about 1.8 times median ocellar diameter; clypeus about 1.7 times broader than long; gena about 0.5 times width of compound eye in profile; scape 3.2 times longer than broad; antennal flagellum more than three times longer than scape; pedicel about as long as broad; first flagellomere about twice as long as second, slightly longer than third. Inner metatibial spur straight, ciliate as in outer spur. Sixth to eighth sterna and genital capsule as in figures 22–28. Color generally as in female except legs and metasoma largely dark brown to black. Pubescence shorter and sparser than in female, except as follows: clypeus and inferior paraocular area with dense, minutely branched, silver hairs; legs and metasoma with whitish hairs; discs of second and third metasomal terga with short (at most one-third median ocellar diameter), simple, erect hairs. Integument with coarser and denser punctures than in female, particularly on head and metasomal terga. Examined material. COLOMBIA: 3 Ƥ, 13, Magdalena, Santa Marta, on road from Bastidas to Bahía Concha, 11 º 15.874 ’N, 74 º 09.924W; Dec 18, 2011, 99 m., V.H. Gonzalez, P. Sepúlveda (ICN, SEMC). Comments. This species was previously known from the female holotype, which is in somewhat poor condition. The male of L. rosellae agrees in most characters with those of the female, except in the usual secondary sexual features, the shorter, sparser body pubescence and the integument with coarser and denser punctures, particularly on head and metasomal terga.Published as part of Gonzalez, Victor H., Sepúlveda, Paula A. & Griswold, Terry L., 2012, Taxonomic notes on American Heriades Spinola, 1808 and Leioproctus Smith, 1853 (Hymenoptera: Megachilidae, Colletidae), pp. 75-78 in Zootaxa 3591 on page 78, DOI: 10.5281/zenodo.21390
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[Transcript of an interview between Lorena Parlee and Pedro J. Gonzalez, 2]
No full textTranscript of an interview between Lorena Parlee and Pedro J. Gonzalez. A wide column of text continues across five pages, with an "L" or P" printed to the left of each paragraph
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